Article
The Fgfr2 W290R mouse model of Crouzon syndrome.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Sept 2012
Gong S-G
Abstract excerpt
PURPOSE: This study aimed to review and discuss the utility of the Fgfr2 (W290R) mouse mutant as a model of human Crouzon syndrome. METHODS: A review of current and past scientific literature on Fibroblast Growth Factor Receptor-2 (FGFR2) protein domain structure, FGFR mutations associated with human Crouzon syndrome, and phenotypic and molecular changes combined with recent observations and experimental data of...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
